| Literature DB >> 23380113 |
Maria Teresa Cardillo1, Roberta Della Bona, Annalisa Caroli, Anna Lia Valentini, Luigi M Biasucci.
Abstract
Pheochromocytoma is a rare tumor that usually develops ahead of the neuroectodermal chromaffin cells of the adrenal medulla, but it may arise anywhere within plexus of sympathetic adrenergic nerves. Headache, palpitations, tremor, excessive sweating, abdominal pain, and hypertensive paroxysm are the common clinical presentations of the tumor, but it has also been reported several cardiac symptoms.Entities:
Mesh:
Year: 2013 PMID: 23380113 DOI: 10.1016/j.ajem.2012.11.019
Source DB: PubMed Journal: Am J Emerg Med ISSN: 0735-6757 Impact factor: 2.469